http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6432965-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8c8dbcf50fe783c0e155cbd9cc1d92c5
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-54
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-54
filingDate 2000-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2002-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c133f0eafb63b19497420f8063d5d4b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c14a8d6ba5e991a1cc44d74ea87af5d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7729044d5249df4783aaf82de98fbc3a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63d29ecef257facafb2941508078fd0b
publicationDate 2002-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6432965-B1
titleOfInvention Fungicidal combinations comprising thieno(2,3-d)pyrimidin-4-one
abstract The invention relates to novel fungicidal compositions having a synergistically increased action, wherein component a) is a thieno[2,3-d]pyrimidin-4-one of formula Iwherein R1 is halogen, R2 is C1-C5alkyl, -CH2-cyclopropyl and R3 is C1-C5alkyl, -CH2-cyclopropyl; in association with b) either an anilinopyrimidine fungicide (II), or an azole fungicide (III), or a morpholine fungicide (IV), or a strobilurin compound (V), or a pyrrole compound (VI), or a phenylamide (VII), or a dithiocarbamate fungicide selected from mancozeb, maneb, metiram and zineb, or a copper compound selected from copper hydroxide, coopper oxychloride, copper sulfate and oxine-copper, or a phthalimide compound (VIII), or prochloraz, or triflumizole, or pyrifenox, or acibenzolar-S-methyl, or chlorothalonil, or cymoxanil, or dimethomorph, or famoxadone, or fenhexamide, or fenarimol, or fluazinam, or fosetyl-aluminium, orquinoxyfen, or fenpropidine, or spiroxamine, or carbendazime, or thlabendazole, or ethirimol, or triazoxide, or guazatine.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2003195225-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7022712-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007043070-A1
priorityDate 1997-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID338
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID13684
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421396321
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129046775
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419569822
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415877725
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID160003548
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID121825
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411962553
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6328269
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID3988
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID243
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415790627
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID3712
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128069423
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID135424354
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID136247704
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226416479
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86298
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2808547
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID142106943
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129247267
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419549912
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226410353
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http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID3988
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Total number of triples: 658.